Search research articles
Contact Us
Filters
Showing results (11-20 of 84) with videos related to
Page
of 9
Sort By:
Cellular and Molecular Life Sciences : CMLS
|
November 30, 2019
Sperm defects in primary ciliary dyskinesia and related causes of male infertility
Anu Sironen, Amelia Shoemark, Mitali Patel, et al.
Brain : a Journal of Neurology
|
July 9, 2004
CLN3L, a novel protein related to the Batten disease protein, is overexpressed in Cln3-/- mice and in Batten disease
Srinivas B Narayan, Johanne V Pastor, Hannah M Mitchison, et al.
Eneuro
|
May 22, 2018
Altered Cerebellar Short-Term Plasticity but No Change in Postsynaptic AMPA-Type Glutamate Receptors in a Mouse Model of Juvenile Batten Disease
Dorota Studniarczyk, Elizabeth L Needham, Hannah M Mitchison, et al.
Journal of Neurochemistry
|
September 18, 2007
Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissue
Sandra Pohl, Hannah M Mitchison, Alfried Kohlschütter, et al.
Molecular Genetics and Metabolism
|
February 1, 2003
Functional categorization of gene expression changes in the cerebellum of a Cln3-knockout mouse model for Batten disease
Andrew I Brooks, Subrata Chattopadhyay, Hannah M Mitchison, et al.
Archives of Disease in Childhood
|
April 29, 2014
Diagnosis and management of primary ciliary dyskinesia
Jane S Lucas, Andrea Burgess, Hannah M Mitchison, et al.
BMC Pulmonary Medicine
|
December 3, 2003
Primary ciliary dyskinesia (Siewert's/Kartagener's syndrome): respiratory symptoms and psycho-social impact
I Christopher McManus, Hannah M Mitchison, Eddie M K Chung, et al.
Traffic (Copenhagen, Denmark)
|
September 27, 2008
Loss of the Batten disease gene CLN3 prevents exit from the TGN of the mannose 6-phosphate receptor
Daniel J Metcalf, Alessandra A Calvi, Matthew Nj Seaman, et al.
Annals of Human Genetics
|
January 15, 2010
Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families
Orit Reish, Montgomery Slatkin, Daphne Chapman-Shimshoni, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 30, 2020
PCD Detect: enhancing ciliary features through image averaging and classification
Amelia Shoemark, Andreia L Pinto, Mitali P Patel, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 84) with videos related to
Sort By:
Page
of 9
Cellular and Molecular Life Sciences : CMLS
|
November 30, 2019
Sperm defects in primary ciliary dyskinesia and related causes of male infertility
Anu Sironen, Amelia Shoemark, Mitali Patel, et al.
Brain : a Journal of Neurology
|
July 9, 2004
CLN3L, a novel protein related to the Batten disease protein, is overexpressed in Cln3-/- mice and in Batten disease
Srinivas B Narayan, Johanne V Pastor, Hannah M Mitchison, et al.
Eneuro
|
May 22, 2018
Altered Cerebellar Short-Term Plasticity but No Change in Postsynaptic AMPA-Type Glutamate Receptors in a Mouse Model of Juvenile Batten Disease
Dorota Studniarczyk, Elizabeth L Needham, Hannah M Mitchison, et al.
Journal of Neurochemistry
|
September 18, 2007
Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissue
Sandra Pohl, Hannah M Mitchison, Alfried Kohlschütter, et al.
Molecular Genetics and Metabolism
|
February 1, 2003
Functional categorization of gene expression changes in the cerebellum of a Cln3-knockout mouse model for Batten disease
Andrew I Brooks, Subrata Chattopadhyay, Hannah M Mitchison, et al.
Archives of Disease in Childhood
|
April 29, 2014
Diagnosis and management of primary ciliary dyskinesia
Jane S Lucas, Andrea Burgess, Hannah M Mitchison, et al.
BMC Pulmonary Medicine
|
December 3, 2003
Primary ciliary dyskinesia (Siewert's/Kartagener's syndrome): respiratory symptoms and psycho-social impact
I Christopher McManus, Hannah M Mitchison, Eddie M K Chung, et al.
Traffic (Copenhagen, Denmark)
|
September 27, 2008
Loss of the Batten disease gene CLN3 prevents exit from the TGN of the mannose 6-phosphate receptor
Daniel J Metcalf, Alessandra A Calvi, Matthew Nj Seaman, et al.
Annals of Human Genetics
|
January 15, 2010
Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families
Orit Reish, Montgomery Slatkin, Daphne Chapman-Shimshoni, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
September 30, 2020
PCD Detect: enhancing ciliary features through image averaging and classification
Amelia Shoemark, Andreia L Pinto, Mitali P Patel, et al.
Page
of 9